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Research 91–120 of 1000+
- 305 Overlaps between inflammatory dermatoses and ichthyoses: need for novel therapeutic approaches
- Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities
- Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes
- Netherton syndrome: effect on ichthyosis linearis circumflexa with dupilumab
- SRD5A3 Is Required for Converting Polyprenol to Dolichol and Is Mutated in a Congenital Glycosylation Disorder
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Hair Loss in Children
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Dermatopathology and molecular genetics
- Hair Loss in Children
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Differential diagnosis of alopetia in children and adolescents
- Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome
- The urine as a diagnostic key for a homozygous EGFR mutation
- Uso actual de la vitamina D en dermatología
- ИХТИОЗ АРЛЕКИНО: КЛИНИЧЕСКИЙ СЛУЧАЙ
- Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix
- Keratin disorders: from gene to therapy
- Cutaneous Syndromes Produced as Side Effects of Triparanol Therapy
- Oral Retinoids in Dermatology
- Chemotherapy of psoriasis and other skin disorders with oral retinoids
- Ulerythema ophryogenes with multiple congenital anomalies
- Common Dermatologic Disorders in Down Syndrome: Systematic Review
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- A STUDY ON CUTANEOUS MANIFESTATIONS OF HYPOTHYROIDISM IN A TERTIARY HOSPITAL IN SOUTH INDIA
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- PHILADELPHIA DERMATOLOGICAL SOCIETY